chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 31462060 31462061 T C 13 GENIC homozygous 116546588 10 31468013 31468014 A G 18 GENIC homozygous 126379922 10 31474667 31474668 A T 5 GENIC homozygous 116546600 10 31486026 31486027 T C 14 GENIC homozygous 116546602 10 31486090 31486091 G A 19 GENIC homozygous 116546604 10 31486805 31486806 T G 19 GENIC homozygous 116752477 10 31487119 31487120 C T 20 GENIC homozygous 116546606 10 31487600 31487601 G A 8 GENIC homozygous 116546608 10 31487731 31487732 C T 28 GENIC homozygous 116546610 10 31488533 31488534 A G 9 GENIC homozygous 116546612 10 31488690 31488691 G A 18 GENIC homozygous 116546614 10 31488718 31488719 G T 20 GENIC homozygous 116546616 10 31488963 31488964 C G 30 GENIC homozygous 116546618 10 31489047 31489048 G A 26 GENIC homozygous 116546620 10 31489167 31489168 A G 6 GENIC homozygous 116546622 10 31489661 31489662 C T 24 GENIC homozygous 116546624 10 31490129 31490130 A G 18 GENIC homozygous 116546626 10 31491221 31491222 T G 16 GENIC homozygous 116546628 10 31491235 31491236 C T 17 GENIC homozygous 116546630 10 31491663 31491664 G A 7 GENIC homozygous 116752479 10 31492144 31492145 G A 22 GENIC homozygous 116546632 10 31492547 31492548 T C 22 GENIC homozygous 116546634 10 31492905 31492906 C T 13 GENIC homozygous 116546636 10 31493055 31493056 A G 17 GENIC homozygous 116546638 10 31493133 31493134 G A 15 GENIC homozygous 116546640